A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569625



Internal ID20942696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134775551..134776218hg38UCSC Ensembl
chr5:134111241..134111908hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267350
Samples
Known GenesDDX46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569625
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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